Zhou G, Seibenhener M L, Wooten M W
Department of Zoology, Auburn University, Auburn, Alabama 36849-5414, USA.
J Biol Chem. 1997 Dec 5;272(49):31130-7. doi: 10.1074/jbc.272.49.31130.
We have previously shown that protein kinase C (PKC)-zeta is activated and required for nerve growth factor (NGF)-induced differentiation of rat pheochromocytoma PC12 cells (Wooten, M. W., Zhou, G., Seibenhener, M. L., and Coleman, E. S. (1994) Cell Growth & Diff. 5, 395-403; Coleman, E. S., and Wooten, M. W. (1994) J. Mol. Neurosci. 5, 39-57). Here we report the characterization and identification of a 106-kDa nuclear protein as a specific substrate of PKC-zeta. NGF treatment of PC12 cells resulted in translocation of PKC-zeta and coincident phosphorylation of a protein that was localized within the nucleoplasm of nuclei isolated from PC12 cells. Addition of PKC-zeta pseudosubstrate peptide in vitro or myristoylated peptide in vivo diminished phosphorylation of pp106 in a dose-dependent fashion. Likewise, addition of purified PKC-zeta, but neither PKC-alpha nor delta, to nuclear extracts resulted in an incremental increase in the phosphorylation of pp106. Expression of dominant-negative PKC-zeta inhibited NGF-induced phosphorylation of pp106, by comparison overexpression of PKC-zeta enhanced basal phosphorylation without a noticeable effect upon NGF-induced effects. Amino acid sequence analysis of four peptides derived from purified pp106 revealed that this protein was homologous to nucleolin. Using an in vitro reconstitution system, purified nucleolin was likewise shown to be phosphorylated by purified PKC-zeta. The staining intensity of both enzyme and substrate in the nucleus increased upon treatment with NGF. In vivo labeling with 32Pi and stimulation of PC12 cells with NGF followed by immunoprecipitation with anti-nucleolin antibody corroborated the in vitro approach documenting enhanced phosphorylation of nucleolin by NGF treatment. Taken together, the findings presented herein document that nucleolin is a target of PKC-zeta that serves to relay NGF signals from cell surface to nucleus in PC12 cells.
我们先前已表明,蛋白激酶C(PKC)-ζ被激活,且是神经生长因子(NGF)诱导大鼠嗜铬细胞瘤PC12细胞分化所必需的(伍滕,M.W.,周,G.,塞本纳纳,M.L.,和科尔曼,E.S.(1994年)《细胞生长与分化》5,395 - 403;科尔曼,E.S.,和伍滕,M.W.(1994年)《分子神经科学杂志》5,39 - 57)。在此我们报告鉴定出一种106 kDa的核蛋白作为PKC-ζ的特异性底物。用NGF处理PC12细胞导致PKC-ζ易位,同时一种定位于从PC12细胞分离的细胞核核质内的蛋白发生磷酸化。在体外添加PKC-ζ假底物肽或在体内添加肉豆蔻酰化肽以剂量依赖方式减少了pp106的磷酸化。同样,向核提取物中添加纯化的PKC-ζ,而非PKC-α或δ,导致pp106的磷酸化呈递增增加。显性负性PKC-ζ的表达抑制了NGF诱导的pp106磷酸化,相比之下,PKC-ζ的过表达增强了基础磷酸化,但对NGF诱导的效应无明显影响。对从纯化的pp106获得的四个肽段进行氨基酸序列分析表明,该蛋白与核仁素同源。使用体外重组系统,同样显示纯化的核仁素可被纯化的PKC-ζ磷酸化。用NGF处理后,细胞核中酶和底物的染色强度均增加。用32Pi进行体内标记并用NGF刺激PC12细胞,随后用抗核仁素抗体进行免疫沉淀,证实了体外实验方法,即证明NGF处理可增强核仁素的磷酸化。综上所述,本文的研究结果表明核仁素是PKC-ζ的作用靶点,其在PC12细胞中起到将NGF信号从细胞表面传递至细胞核的作用。